Canonical Allele Identifier: CA2676968869

Gene: FLT4

Linked Data

• gnomAD v4: 5-180609911-G-GTACCAC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180609911_180609912insTACCAC , CM000667.2:g.180609911_180609912insTACCAC	GRCh38
NC_000005.9:g.180036911_180036912insTACCAC , CM000667.1:g.180036911_180036912insTACCAC	GRCh37
NC_000005.8:g.179969517_179969518insTACCAC	NCBI36
NG_011536.1:g.44713_44714insGTGGTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3800_3801insGTGGTA MANE Select	ENSP00000261937.6:p.Gly1267_Ser1268insTrpTyr
ENST00000261937.10:c.3800_3801insGTGGTA	ENSP00000261937.6:p.Gly1267_Ser1268insTrpTyr
ENST00000393347.7:c.3800_3801insGTGGTA	ENSP00000377016.3:p.Gly1267_Ser1268insTrpTyr
ENST00000502603.5:n.500_501insGTGGTA
ENST00000502649.5:c.3800_3801insGTGGTA	ENSP00000426057.1:p.Gly1267_Ser1268insTrpTyr
ENST00000507059.5:n.4150_4151insGTGGTA
ENST00000619105.4:c.*2743_*2744insGTGGTA	ENSP00000481134.1:n.*2743_*2744insGTGGTA
NM_002020.4:c.3800_3801insGTGGTA	NP_002011.2:p.Gly1267_Ser1268insTrpTyr
NM_182925.4:c.3800_3801insGTGGTA	NP_891555.2:p.Gly1267_Ser1268insTrpTyr
XM_011534477.1:c.4049_4050insGTGGTA	XP_011532779.1:p.Gly1350_Ser1351insTrpTyr
XM_011534478.1:c.4031_4032insGTGGTA	XP_011532780.1:p.Gly1344_Ser1345insTrpTyr
XM_011534479.1:c.4049_4050insGTGGTA	XP_011532781.1:p.Gly1350_Ser1351insTrpTyr
XM_011534480.1:c.4049_4050insGTGGTA	XP_011532782.1:p.Gly1350_Ser1351insTrpTyr
XM_011534481.1:c.4049_4050insGTGGTA	XP_011532783.1:p.Gly1350_Ser1351insTrpTyr
XM_011534482.1:c.3818_3819insGTGGTA	XP_011532784.1:p.Gly1273_Ser1274insTrpTyr
XM_011534483.1:c.3740_3741insGTGGTA	XP_011532785.1:p.Gly1247_Ser1248insTrpTyr
XM_011534484.1:c.3341_3342insGTGGTA	XP_011532786.1:p.Gly1114_Ser1115insTrpTyr
XR_941095.1:n.4086_4087insGTGGTA
NM_001354989.1:c.3800_3801insGTGGTA	NP_001341918.1:p.Gly1267_Ser1268insTrpTyr
XM_011534478.3:c.4031_4032insGTGGTA	XP_011532780.1:p.Gly1344_Ser1345insTrpTyr
XM_011534484.2:c.3341_3342insGTGGTA	XP_011532786.1:p.Gly1114_Ser1115insTrpTyr
XM_017009263.1:c.4031_4032insGTGGTA	XP_016864752.1:p.Gly1344_Ser1345insTrpTyr
XM_017009264.2:c.4031_4032insGTGGTA	XP_016864753.1:p.Gly1344_Ser1345insTrpTyr
XM_017009265.1:c.4031_4032insGTGGTA	XP_016864754.1:p.Gly1344_Ser1345insTrpTyr
XM_017009266.1:c.4031_4032insGTGGTA	XP_016864755.1:p.Gly1344_Ser1345insTrpTyr
XM_017009267.2:c.4031_4032insGTGGTA	XP_016864756.1:p.Gly1344_Ser1345insTrpTyr
XM_017009268.1:c.3722_3723insGTGGTA	XP_016864757.1:p.Gly1241_Ser1242insTrpTyr
XR_001742050.2:n.4290_4291insGTGGTA
NM_182925.5:c.3800_3801insGTGGTA MANE Select	NP_891555.2:p.Gly1267_Ser1268insTrpTyr
NM_001354989.2:c.3800_3801insGTGGTA	NP_001341918.1:p.Gly1267_Ser1268insTrpTyr
NM_002020.5:c.3800_3801insGTGGTA	NP_002011.2:p.Gly1267_Ser1268insTrpTyr